PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR Adverse Event — Injury (MDR 3006705815-2020-01726)
PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR Adverse Event — Injury (MDR 3006705815-2020-01726) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR; Generic name: SCS IPG; Manufacturer: ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, L
| Device | PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR |
|---|---|
| Generic name | SCS IPG |
| Manufacturer | ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC) |
| Report number | 3006705815-2020-01726 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, CONSUM |
| Narrative | THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICE WAS NOT RETURNED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED. |
| Source | openFDA MAUDE (device adverse events) |
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